[go: up one dir, main page]

WO2016074225A1 - Procédé de résolution de l'intermédiaire du citalopram 5-cyanogéne diol - Google Patents

Procédé de résolution de l'intermédiaire du citalopram 5-cyanogéne diol Download PDF

Info

Publication number
WO2016074225A1
WO2016074225A1 PCT/CN2014/091139 CN2014091139W WO2016074225A1 WO 2016074225 A1 WO2016074225 A1 WO 2016074225A1 CN 2014091139 W CN2014091139 W CN 2014091139W WO 2016074225 A1 WO2016074225 A1 WO 2016074225A1
Authority
WO
WIPO (PCT)
Prior art keywords
ether
solvent
resolution
peak
ethylene glycol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/CN2014/091139
Other languages
English (en)
Chinese (zh)
Inventor
梁尊俊
胡斯琪
彭才华
黄文峰
芦启锋
涂国良
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zhejiang Huahai Pharmaceutical Co Ltd
Original Assignee
Zhejiang Huahai Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zhejiang Huahai Pharmaceutical Co Ltd filed Critical Zhejiang Huahai Pharmaceutical Co Ltd
Priority to ES14905690T priority Critical patent/ES2881105T3/es
Priority to US15/521,776 priority patent/US10287240B2/en
Priority to PCT/CN2014/091139 priority patent/WO2016074225A1/fr
Priority to CN201480081785.8A priority patent/CN107074750B/zh
Priority to EP14905690.5A priority patent/EP3219702B1/fr
Publication of WO2016074225A1 publication Critical patent/WO2016074225A1/fr
Anticipated expiration legal-status Critical
Priority to US16/282,922 priority patent/US10508076B2/en
Ceased legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00—Preparation of carboxylic acid nitriles
    • C07C253/32—Separation; Purification; Stabilisation; Use of additives
    • C07C253/34—Separation; Purification
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/50—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
    • C07C255/59—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C07C69/78—Benzoic acid esters
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Definitions

  • the present invention relates to a process for the resolution of citalopram intermediate 5-cyanodiol.
  • Citalopram is an important class of antidepressant drugs, a selective 5-hydroxytryptamine (5-HT) reuptake S-constitutive inhibitor, its single optically active isomer, dextroamphetamine (S-citalopram) is 100 times more potent than its anti-depressant effect, R-citalopram, and therefore has better efficacy and less dosage.
  • 5-HT 5-hydroxytryptamine
  • S-citalopram dextroamphetamine
  • R-citalopram anti-depressant effect
  • the S-type isomers are mainly sold in the European and American markets, which are prepared by cyclization and salt formation of S-5-cyanodiol (IV).
  • (S)-5-Cyanamide (IV) is a key starting material for the production of S-citalopram.
  • it is generally composed of racemic 5-cyanodiol (I) and resolving agent D-( +) Di-p-toluoyl tartaric acid (II) (abbreviated as DPTTA), salt-forming and crystallization separation in an alcohol and an alcohol-containing mixed solvent (S)-5-Cyanide diol resolution intermediate (III) ), and then prepared by alkali free preparation.
  • DPTTA Di-p-toluoyl tartaric acid
  • S -5-Cyanide diol resolution intermediate
  • the splitting process can be expressed as follows:
  • the structure of the resolving agent DPTTA is as follows:
  • a first aspect of the present invention provides an efficient method for the resolution of 5-cyanodiol (I) comprising the steps of: crystallizing (S)-4-[4- represented by Formula IV in a solvent to be resolved Dimethylamino-1-(4-fluorophenyl)-1-hydroxybutyl]-3-hydroxymethylbenzonitrile is formed with the resolving agent D-(+) di-p-toluoyl tartaric acid represented by Formula II a salt; wherein the dissolving solvent is an ether solvent;
  • the ether solvent is selected from the group consisting of: tetrahydrofuran, methyltetrahydrofuran, cyclopentyl methyl ether, diisopropyl ether, dioxane, ethylene glycol monomethyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, and ethyl Diol dibutyl ether, diethylene glycol dimethyl ether, propylene glycol dimethyl ether and propylene glycol diethyl ether.
  • the ether solvent preferably contains a certain amount of water, and the volume percentage of water in the solvent is 0.2% to 10%, and the volume percentage of water is further preferably 0.2% to 5%.
  • the crystalline particles of the intermediate are more regular and have a large particle size, which is very easy to filter and is more convenient to handle in production.
  • thermogravimetric analysis (TGA) spectra are shown in Figure 4.
  • the Form C powder X-ray diffraction (PXRD) spectrum is shown in Figure 5.
  • the diffraction peak angle and intensity data are shown in Table 1 below:
  • the (S)-5-cyanodiol-resolved intermediates Form B and Form C prepared by the present invention are different from the crystal structure of the (S)-5-cyanodiol-resolved intermediate obtained by the prior art.
  • a single aqueous or anhydrous solvent can be used, the solvent recovery rate is high, and the production cost is low;
  • D-(+) di-p-toluoyl tartaric acid was added (15.0 g) to n-propanol (118 ml), and the mixture was heated to 40 ° C, stirred and dissolved, and acetic acid (1.2 g) was added.
  • the solution of the above-mentioned resolving agent was added to a solution of racemic 5-cyanodiol base (34.2 g) and n-propanol (32 ml) over 1 hour, kept at 40 ° C, and stirred for 2 hours. Cool down at 20-25 ° C, stir and crystallize for 2 hours. Filtration, the filter cake was rinsed twice with n-propanol to obtain a crude chiral purity of the crude intermediate: S-5-cyanodiol 91% to 98%.
  • the crude product was reintroduced into the flask, n-propanol (86 ml) was added, and the mixture was warmed to 50 ° C and stirred for 2 hours. Then, the mixture was cooled at 20 to 25 ° C, and the mixture was incubated and incubated for 2 hours. Filtration, the filter cake was rinsed once with n-propanol, and the filter cake was vacuum dried at 50 ° C to obtain 18.5 g of the intermediate. The yield was 34.5%. The chiral purity of the obtained split intermediate was: S-5-cyanodiol 99.3%.
  • the racemic 5-cyanodiol (178.1 g) was added, and isopropyl alcohol (1125 ml) was added thereto, and the mixture was heated to 50 to 55 ° C, and stirred to dissolve.
  • the temperature was controlled at 50 to 55 ° C, D-(+) di-p-toluoyl tartaric acid (105 g,) was added, and the temperature was slowly lowered to 25 to 30 ° C, and the mixture was stirred for 10 hours. Filtration, the filter cake was rinsed twice with isopropanol, and the amount of each wash was 110 ml.
  • the filter cake is vacuum dried at 50 ° C to obtain the intermediate
  • the crude product was 185 g, and the chiral purity was: S-5-cyanodiol 96.1%.
  • the crude product was re-introduced into the flask, and isopropyl alcohol (1500 ml) was added thereto, and the mixture was heated to 80 ° C and stirred to dissolve. Then, it was cooled at 20 to 25 ° C, and the mixture was incubated for 1 hour while being kept warm. Filtration, the filter cake was rinsed twice with isopropyl alcohol, 50 ml each time, and the filter cake was vacuum dried at 50 ° C to obtain 101.2 g of the intermediate. The yield was 36.3%, and the chiral purity was: S- 5-cyanodiol 99.1%.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention concerne un procédé de résolution de formule 4- [4-diméthylamino -1- (4-fluorophényl)-1-hydroxylbutyl]-3-hydroxyméthyl cyanophényle sous la forme d'un énantiomère de celui-ci, comprenant les étapes suivantes consistant à : cristalliser, dans un solvant de résolution, un sel formé à partir de (S)-4-[4-diméthylamino-1-(4-fluorophényl)-1-hydroxylbutyl]-3-hydroxyméthyl cyanophényle et un agent de résolution acide D- (+) di-p-toluoyl tartrique; le procédé est caractérisé en ce que le solvant de résolution est un solvant à base d'éther. L'invention concerne également une nouvelle forme cristalline de l'intermédiaire résolu.
PCT/CN2014/091139 2014-11-14 2014-11-14 Procédé de résolution de l'intermédiaire du citalopram 5-cyanogéne diol Ceased WO2016074225A1 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
ES14905690T ES2881105T3 (es) 2014-11-14 2014-11-14 Método para la resolución del producto intermedio de citalopram 5-cianodiol
US15/521,776 US10287240B2 (en) 2014-11-14 2014-11-14 Method for resolution of citalopram intermediate 5-cyano diol
PCT/CN2014/091139 WO2016074225A1 (fr) 2014-11-14 2014-11-14 Procédé de résolution de l'intermédiaire du citalopram 5-cyanogéne diol
CN201480081785.8A CN107074750B (zh) 2014-11-14 2014-11-14 一种拆分西酞普兰中间体5-氰二醇的方法
EP14905690.5A EP3219702B1 (fr) 2014-11-14 2014-11-14 Procédé de résolution de l'intermédiaire du citalopram 5-cyanogéne diol
US16/282,922 US10508076B2 (en) 2014-11-14 2019-02-22 Method for resolution of citalopram intermediate 5-cyano diol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2014/091139 WO2016074225A1 (fr) 2014-11-14 2014-11-14 Procédé de résolution de l'intermédiaire du citalopram 5-cyanogéne diol

Related Child Applications (3)

Application Number Title Priority Date Filing Date
US15/521,776 A-371-Of-International US10287240B2 (en) 2014-11-14 2014-11-14 Method for resolution of citalopram intermediate 5-cyano diol
US16/282,922 Continuation US10508076B2 (en) 2014-11-14 2019-02-22 Method for resolution of citalopram intermediate 5-cyano diol
US16/282,922 Division US10508076B2 (en) 2014-11-14 2019-02-22 Method for resolution of citalopram intermediate 5-cyano diol

Publications (1)

Publication Number Publication Date
WO2016074225A1 true WO2016074225A1 (fr) 2016-05-19

Family

ID=55953616

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2014/091139 Ceased WO2016074225A1 (fr) 2014-11-14 2014-11-14 Procédé de résolution de l'intermédiaire du citalopram 5-cyanogéne diol

Country Status (5)

Country Link
US (2) US10287240B2 (fr)
EP (1) EP3219702B1 (fr)
CN (1) CN107074750B (fr)
ES (1) ES2881105T3 (fr)
WO (1) WO2016074225A1 (fr)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006106531A1 (fr) * 2005-04-04 2006-10-12 Jubilant Organosys Ltd Processus de preparation d'escitalopram ou de ses sels d'addition acides
WO2007012954A1 (fr) * 2005-07-27 2007-02-01 Aurobindo Pharma Limited Procédé amélioré pour la préparation d'escitalopram
CN101265215A (zh) * 2008-04-18 2008-09-17 浙江奥托康制药集团股份有限公司 一种右旋西酞普兰中间体s-型二醇的制备方法
CN101386583A (zh) * 2007-09-11 2009-03-18 H.隆德贝克有限公司 制备依地普伦的方法
WO2010004575A2 (fr) * 2008-06-16 2010-01-14 Shodhana Laboratories Limited Préparation de l’escitalopram, ses sels et ses intermédiaires
CN102190600A (zh) * 2010-03-13 2011-09-21 浙江华海药业股份有限公司 一种右旋西酞普兰中间体s-型二醇的制备方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8814057D0 (en) * 1988-06-14 1988-07-20 Lundbeck & Co As H New enantiomers & their isolation
GB0601286D0 (en) * 2006-01-23 2006-03-01 Sandoz Ag Asymmetric synthesis
WO2008059514A2 (fr) * 2006-07-31 2008-05-22 Cadila Healthcare Limited Procédé de préparation d'escitalopram
JP5256749B2 (ja) * 2008-01-23 2013-08-07 住友化学株式会社 乳剤組成物

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006106531A1 (fr) * 2005-04-04 2006-10-12 Jubilant Organosys Ltd Processus de preparation d'escitalopram ou de ses sels d'addition acides
WO2007012954A1 (fr) * 2005-07-27 2007-02-01 Aurobindo Pharma Limited Procédé amélioré pour la préparation d'escitalopram
CN101386583A (zh) * 2007-09-11 2009-03-18 H.隆德贝克有限公司 制备依地普伦的方法
CN101265215A (zh) * 2008-04-18 2008-09-17 浙江奥托康制药集团股份有限公司 一种右旋西酞普兰中间体s-型二醇的制备方法
WO2010004575A2 (fr) * 2008-06-16 2010-01-14 Shodhana Laboratories Limited Préparation de l’escitalopram, ses sels et ses intermédiaires
CN102190600A (zh) * 2010-03-13 2011-09-21 浙江华海药业股份有限公司 一种右旋西酞普兰中间体s-型二醇的制备方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP3219702A4 *

Also Published As

Publication number Publication date
US10287240B2 (en) 2019-05-14
US20190185418A1 (en) 2019-06-20
EP3219702A4 (fr) 2018-05-30
EP3219702A1 (fr) 2017-09-20
ES2881105T3 (es) 2021-11-26
EP3219702B1 (fr) 2021-05-05
US20170240505A1 (en) 2017-08-24
CN107074750B (zh) 2022-03-25
CN107074750A (zh) 2017-08-18
US10508076B2 (en) 2019-12-17

Similar Documents

Publication Publication Date Title
JP6378844B2 (ja) 第６結晶形ソホスブビルの調製方法
TW200936574A (en) New process
JP2007516934A (ja) （＋）−（ｓ）−クロピドグレル重硫酸塩形態−ｉの新規な製造方法
WO2024017170A1 (fr) Forme cristalline de s-(-)-nicotine(-)-dibenzoyl-l-tartrate, procédé de préparation et utilisation
EP3424908A1 (fr) Procédé de préparation de levosimendan
JP5826371B2 (ja) ペメトレキセド塩の製造方法
JP4505335B2 (ja) ラセミ体シタロプラムジオール（ｒａｃｅｍｉｃｃｉｔａｌｏｐｒａｍｄｉｏｌ）および／またはＳ−もしくはＲ−シタロプラムジオールの製造方法、およびラセミ体シタロプラム、Ｒ−シタロプラムおよび／またはＳ−シタロプラムを製造するために、上記ジオールを使用する方法。
JP6137185B2 (ja) （ｒ）−１，１，３−トリメチル−４−アミノインダンの製造方法
TWI391383B (zh) 製造艾司西酞普蘭（ｅｓｃｉｔａｌｏｐｒａｍ）之方法
KR20160125115A (ko) 3-히드록시테트라하이드로퓨란의 제조방법
WO2016146049A1 (fr) Procédé de préparation industrielle de midazolam
WO2016074225A1 (fr) Procédé de résolution de l'intermédiaire du citalopram 5-cyanogéne diol
EP1700851B1 (fr) Diol intermediaire du citalopram a l'etat de cristal alcalin
CN102190600A (zh) 一种右旋西酞普兰中间体s-型二醇的制备方法
KR102556971B1 (ko) 데커시놀((+)-Decursinol)의 신규한 제조방법
CN103408495A (zh) 甲磺酸酚妥拉明的合成工艺
JP2010229098A (ja) イソインドリン誘導体のａ型の結晶形の製造方法及びイソインドリン誘導体のａ型の結晶形
CN108586450B (zh) 一种胆碱m受体抗结剂的重结晶纯化方法
CN107793320B (zh) 手性拆分制备单一构型3-氨基-1-丁醇的方法
CN100494162C (zh) 一种非等比例顺式舍曲林盐酸盐混合物的分离方法
JP2016222628A (ja) デュロキセチン塩酸塩の製造方法
CN108610341B (zh) 一种米氮平合成及后处理方法
DK201500520A1 (en) Crystalline forms of (R)-4-[4-(dimethylamino)-1-(4'-fluorophenyl)-hydroxybutyl]-3-(hydroxymethyl)-benzonitrile free base and (S)-4-[4-(dimethylamino)-1-(4'-fluoro-phenyl)-hydroxybutyl]-3-(hydroxymethyl)-benzonitrile free base and of racemic 4-[4-(dimethylamino)-1-(4'-fluorophenyl)-hydroxybutyl]-3-(hydroxyl-methyl)-benzonitrile toluene hemisolvate
JP6815853B2 (ja) （１Ｓ）−４−［４−（ジメチルアミノ）−１−（４’−フルオロフェニル）−１−ヒドロキシブチル］−３−（ヒドロキシメチル）−ベンゾニトリルヘミ（＋）−ジ−（ｐ−トルオイル）酒石酸塩の製造方法、及び該酒石酸塩を用いた（１Ｓ）−１−［３−（ジメチルアミノ）プロピル］−１−（４−フルオロフェニル）−１，３−ジヒドロイソベンゾフラン−５−カルボニトリル及びその塩の製造方法
CN106432253A (zh) 一种维帕他韦新晶型及其制备方法

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 14905690

Country of ref document: EP

Kind code of ref document: A1

REEP Request for entry into the european phase

Ref document number: 2014905690

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2014905690

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 15521776

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE